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O95231 (VENTX_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 95. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Homeobox protein VENTX
Alternative name(s):
VENT homeobox homolog
VENT-like homeobox protein 2
Gene names
Name:VENTX
Synonyms:HPX42B, VENTX2
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length258 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

May be involved in ventralization.

Subcellular location

Nucleus Probable.

Tissue specificity

Expressed in bone marrow of patients recovering from chemotherapy. Also expressed in an erythroleukemia cell line. Ref.1

Sequence similarities

Contains 1 homeobox DNA-binding domain.

Ontologies

Keywords
   Cellular componentNucleus
   Coding sequence diversityPolymorphism
   DomainHomeobox
   LigandDNA-binding
   Molecular functionDevelopmental protein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processmulticellular organismal development

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular componentnucleus

Inferred from electronic annotation. Source: UniProtKB-SubCell

   Molecular functionsequence-specific DNA binding

Inferred from electronic annotation. Source: InterPro

sequence-specific DNA binding transcription factor activity

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 258258Homeobox protein VENTX
PRO_0000305938

Regions

DNA binding91 – 15060Homeobox

Natural variations

Natural variant421L → P. Ref.3
Corresponds to variant rs2240892 [ dbSNP | Ensembl ].
VAR_035243
Natural variant791M → V.
Corresponds to variant rs2240891 [ dbSNP | Ensembl ].
VAR_035244
Natural variant1011E → K.
Corresponds to variant rs2270192 [ dbSNP | Ensembl ].
VAR_049591
Natural variant1911G → R.
Corresponds to variant rs9418952 [ dbSNP | Ensembl ].
VAR_049592
Natural variant2471G → D.
Corresponds to variant rs9418953 [ dbSNP | Ensembl ].
VAR_061269

Sequences

Sequence LengthMass (Da)Tools
O95231 [UniParc].

Last modified May 1, 1999. Version 1.
Checksum: 6F611169122D8244

FASTA25827,552
        10         20         30         40         50         60 
MRLSSSPPRG PQQLSSFGSV DWLSQSSCSG PTHTPRPADF SLGSLPGPGQ TSGAREPPQA 

        70         80         90        100        110        120 
VSIKEAAGSS NLPAPERTMA GLSKEPNTLR APRVRTAFTM EQVRTLEGVF QHHQYLSPLE 

       130        140        150        160        170        180 
RKRLAREMQL SEVQIKTWFQ NRRMKHKRQM QDPQLHSPFS GSLHAPPAFY STSSGLANGL 

       190        200        210        220        230        240 
QLLCPWAPLS GPQALMLPPG SFWGLCQVAQ EALASAGASC CGQPLASHPP TPGRPSLGPA 

       250 
LSTGPRGLCA MPQTGDAF 

« Hide

References

« Hide 'large scale' references
[1]"Molecular cloning of a human Vent-like homeobox gene."
Moretti P.A.B., Davidson A.J., Baker E., Lilley B., Zon L.I., D'Andrea R.J.
Genomics 76:21-29(2001) [PubMed: 11549314] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA], TISSUE SPECIFICITY.
Tissue: Bone marrow.
[2]"The DNA sequence and comparative analysis of human chromosome 10."
Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. expand/collapse author list , Bird C.P., Ainscough R., Almeida J.P., Ashwell R.I.S., Ambrose K.D., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Bates K., Beasley H., Bray-Allen S., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Cahill P., Camire D., Carter N.P., Chapman J.C., Clark S.Y., Clarke G., Clee C.M., Clegg S., Corby N., Coulson A., Dhami P., Dutta I., Dunn M., Faulkner L., Frankish A., Frankland J.A., Garner P., Garnett J., Gribble S., Griffiths C., Grocock R., Gustafson E., Hammond S., Harley J.L., Hart E., Heath P.D., Ho T.P., Hopkins B., Horne J., Howden P.J., Huckle E., Hynds C., Johnson C., Johnson D., Kana A., Kay M., Kimberley A.M., Kershaw J.K., Kokkinaki M., Laird G.K., Lawlor S., Lee H.M., Leongamornlert D.A., Laird G., Lloyd C., Lloyd D.M., Loveland J., Lovell J., McLaren S., McLay K.E., McMurray A., Mashreghi-Mohammadi M., Matthews L., Milne S., Nickerson T., Nguyen M., Overton-Larty E., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K., Rice C.M., Rogosin A., Ross M.T., Sarafidou T., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Standring L., Sycamore N., Tester J., Thorpe A., Torcasso W., Tracey A., Tromans A., Tsolas J., Wall M., Walsh J., Wang H., Weinstock K., West A.P., Willey D.L., Whitehead S.L., Wilming L., Wray P.W., Young L., Chen Y., Lovering R.C., Moschonas N.K., Siebert R., Fechtel K., Bentley D., Durbin R.M., Hubbard T., Doucette-Stamm L., Beck S., Smith D.R., Rogers J.
Nature 429:375-381(2004) [PubMed: 15164054] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT PRO-42.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF068006 mRNA. Translation: AAC82375.1.
AF288039 Genomic DNA. Translation: AAK83043.1.
AL445199 Genomic DNA. Translation: CAI17343.1.
BC108915 mRNA. Translation: AAI08916.1.
BC108916 mRNA. Translation: AAI08917.1.
IPIIPI00004447.
RefSeqNP_055283.1. NM_014468.2.
UniGeneHs.125231.

3D structure databases

HSSPHSSP built from PDB template 1K61 based on UniProtKB Q6B2C0.
ProteinModelPortalO95231.
SMRO95231. Positions 93-149.
ModBaseSearch...

Protein-protein interaction databases

STRINGO95231.

Proteomic databases

PRIDEO95231.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000325980; ENSP00000357556; ENSG00000151650.
GeneID27287.
KEGGhsa:27287.
UCSCuc001lmd.1. human.

Organism-specific databases

CTD27287.
GeneCardsGC10P135051.
H-InvDBHIX0036778.
HIX0201519.
HGNCHGNC:13639. VENTX.
MIM607158. gene.
neXtProtNX_O95231.
PharmGKBPA37803.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG11121.
GeneTreeENSGT00590000083002.
InParanoidO95231.
OMADWLSQSS.
OrthoDBEOG44TP97.
PhylomeDBO95231.

Gene expression databases

ArrayExpressO95231.
BgeeO95231.
CleanExHS_VENTX.
GenevestigatorO95231.

Family and domain databases

InterProIPR001356. Homeobox.
IPR017970. Homeobox_CS.
IPR009057. Homeodomain-like.
IPR012287. Homeodomain-rel.
[Graphical view]
Gene3DG3DSA:1.10.10.60. Homeodomain-rel. 1 hit.
PfamPF00046. Homeobox. 1 hit.
[Graphical view]
SMARTSM00389. HOX. 1 hit.
[Graphical view]
SUPFAMSSF46689. Homeodomain_like. 1 hit.
PROSITEPS00027. HOMEOBOX_1. 1 hit.
PS50071. HOMEOBOX_2. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio50228.
SOURCESearch...

Entry information

Entry nameVENTX_HUMAN
AccessionPrimary (citable) accession number: O95231
Secondary accession number(s): Q32MZ3
Entry history
Integrated into UniProtKB/Swiss-Prot: October 2, 2007
Last sequence update: May 1, 1999
Last modified: January 25, 2012
This is version 95 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 10

Human chromosome 10: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families